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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
<abbrev-journal-title abbrev-type="nlm-ta">Atmos. Chem. Phys.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus Publications</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-2-17-2002</article-id>
<title-group>
<article-title>Modelling the contribution of sea salt and dimethyl sulfide derived aerosol to marine CCN</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yoon</surname>
<given-names>Y. J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Brimblecombe</surname>
<given-names>P.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>School of Environmental Sciences, University of East Anglia, Norwich NR4 7TJ, UK</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Now at: Department of Experimental Physics, National University of Ireland Galway, Galway, Ireland</addr-line>
</aff>
<pub-date pub-type="epub">
<day>14</day>
<month>01</month>
<year>2002</year>
</pub-date>
<volume>2</volume>
<issue>1</issue>
<fpage>17</fpage>
<lpage>30</lpage>
<permissions>
<copyright-statement>Copyright: &#x000a9; 2002 Y. J. Yoon</copyright-statement>
<copyright-year>2002</copyright-year>
<license license-type="open-access">
<license-p>This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Generic License. To view a copy of this licence, visit <ext-link ext-link-type="uri"  xlink:href="https://creativecommons.org/licenses/by-nc-sa/2.5/">https://creativecommons.org/licenses/by-nc-sa/2.5/</ext-link></license-p>
</license>
</permissions>
<self-uri xlink:href="https://acp.copernicus.org/articles/2/17/2002/acp-2-17-2002.html">This article is available from https://acp.copernicus.org/articles/2/17/2002/acp-2-17-2002.html</self-uri>
<self-uri xlink:href="https://acp.copernicus.org/articles/2/17/2002/acp-2-17-2002.pdf">The full text article is available as a PDF file from https://acp.copernicus.org/articles/2/17/2002/acp-2-17-2002.pdf</self-uri>
<abstract>
<p>The concentration of cloud condensation nuclei (CCN) in the marine
      boundary layer (MBL) was estimated from dimethyl sulfide (DMS) flux, sea
      salt (SS)
      emission, and aerosols entrained from the free troposphere (FT). Only under clean air
      conditions, did the nucleation of DMS derived sulfur (DMS CCN) contribute significantly to the MBL CCN.  The accommodation coefficient for sulfuric acid mass
      transfer was found to be a very important parameter in the modeling the contribution
      of DMS to MBL CCN.  The relationship between seawater DMS and MBL CCN was found to be non-linear mainly due to the transfer processes of sulfuric acid onto
      aerosols.  In addition, sea salt derived CCN (SS CCN) and entrained aerosol from the FT
      (FT CCN) affected the MBL CCN directly, by supplying CCN, and indirectly, by
      behaving as an efficient sink for sulfuric acid.  The SS CCN explained more than
      50% of the total predicted MBL CCN when wind speeds were moderate and high.
      Sea salt
      and FT aerosol may often be more efficient sources of MBL CCN than DMS.</p>
</abstract>
<counts><page-count count="14"/></counts>
</article-meta>
</front>
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